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Exciton Technologies, Inc.

FDA Regulatory Profile

Exciton Technologies, Inc. has 0 FDA recalls, 1 inspection, 7 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 18, 2014 · NAI
Latest 510(k)
Dec 6, 2018

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances7Oct 4, 2026Not statedCurrent
Inspections1Oct 23, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 18, 2014Edmonton, CanadaDevicesNo Action Indicated (NAI)3007963765

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K182680KerraContact Ag Perf Advanced Perforated Silver Wound DressingDec 6, 2018
K162508KerraCel Ag Gelling Fiber Silver DressingFeb 13, 2017
K133775EXSALT SD7 WOUND DRESSING WITH ADHESIVE BACKINGMar 26, 2014
K113564EXSALT T7 WOUND DRESSINGDec 15, 2011
K103067EXSALT SD7 WOUND DRESSINGMay 20, 2011
K100580EXSALT WOUND DRESSINGOct 12, 2010
K083870EXSALT SD7 WOUND DRESSINGJul 30, 2009

FDA data resources